基于图形生成和多源信息融合的因果增强型药物-靶点相互作用预测

Guanyu Qiao, Guohua Wang, Yang Li
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引用次数: 0

摘要

动机预测药物与靶点的相互作用是生物医学领域的一项重要任务,有助于发现潜在的药物分子靶点,开发疗效更高、副作用更小的靶向治疗方法。虽然目前有多种基于异构信息网络的药物-靶点相互作用(DTI)预测方法,但这些方法在捕捉药物与靶点之间的基本相互作用和确保模型的可解释性方面面临挑战。此外,它们还需要人为地构建元路径或大量的特征工程(先验知识),而图生成可以更灵活地融合信息,无需元路径选择:我们提出了一种药物-靶点相互作用因果增强预测方法(CE-DTI),它整合了图生成和多源信息融合。首先,我们通过自动生成图,建立多源信息融合模型来表示药物和靶标。一旦药物和靶标结合在一起,就会构建一个药物-靶标配对网络,从而将药物-靶标相互作用预测转化为一个节点分类问题。具体来说,周围节点对中心节点的影响被分为两类:因果变量节点和非因果变量节点。因果变量节点会对中心节点的分类产生重大影响,而非因果变量节点则不会。然后利用因果不变性来增强药物-目标配对网络的对比学习。在多个数据集上,我们的方法与其他具有竞争力的基准方法相比表现出了卓越的性能。同时,实验结果还表明,因果增强策略可以探索 DTPs 之间的潜在因果效应,并发现新的潜在靶点。此外,案例研究也证明了这种方法可以识别潜在的药物靶点:AdaDR的源代码可在以下网址获得:Https://github.com/catly/CE-DTI.
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Causal enhanced drug-target interaction prediction based on graph generation and multi-source information fusion.

Motivation: The prediction of drug-target interaction is a vital task in the biomedical field, aiding in the discovery of potential molecular targets of drugs and the development of targeted therapy methods with higher efficacy and fewer side effects. Although there are various methods for drug-target interaction (DTI) prediction based on heterogeneous information networks, these methods face challenges in capturing the fundamental interaction between drugs and targets and ensuring the interpretability of the model. Moreover, they need to construct meta-paths artificially or a lot of feature engineering (prior knowledge), and graph generation can fuse information more flexibly without meta-path selection.

Results: We propose a causal enhanced method for drug-target interaction (CE-DTI) prediction that integrates graph generation and multi-source information fusion. First, we represent drugs and targets by modeling the fusion of their multi-source information through automatic graph generation. Once drugs and targets are combined, a network of drug-target pairs is constructed, transforming the prediction of drug-target interactions into a node classification problem. Specifically, the influence of surrounding nodes on the central node is separated into two groups: causal and non-causal variable nodes. Causal variable nodes significantly impact the central node's classification, while non-causal variable nodes do not. Causal invariance is then used to enhance the contrastive learning of the drug-target pairs network. Our method demonstrates excellent performance compared with other competitive benchmark methods across multiple datasets. At the same time, the experimental results also show that the causal enhancement strategy can explore the potential causal effects between DTPs, and discover new potential targets. Additionally, case studies demonstrate that this method can identify potential drug targets.

Availability and implementation: The source code of AdaDR is available at: https://github.com/catly/CE-DTI.

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